Fluoroscopic Endobutton in Clavicle Fractures and AC Dislocations

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorBOUCHRA BENKESSOU

About this trial

This study aims to inform clinical decision-making by thoroughly examining the outcomes of different treatment approaches for lateral quarter clavicle fractures and acromioclavicular dislocations. By evaluating the safety and efficacy of Knotless AC TightRope® repair devices and comparing short- and long-term results with other fixation techniques, the investigators hope to contribute to the improvement of treatment protocols for these common shoulder injuries. This research could significantly impact patients' quality of life by enabling optimal recovery and restoration of shoulder function.

Eligibility criteria

Qualifiers

Patients presenting with a fracture of the lateral quarter of the clavicle or a severe acromioclavicular disjunction (Rockwood stages III-V) confirmed by radiological examination

Patients who have given their consent to participate in the observational study after being informed by the surgeon

Disqualifiers

Minor patients;

Subjects who are legally protected adults, under guardianship or trusteeship;

Infection;

Pregnant or breastfeeding women.

Trial design

Treatments tested in this trial

  • endobutton under fluoroscopic control (Knotless AC TightRope®)

Treatment groups

10 Participants
are divided into 1 treatment group

Sponsors and collaborators

BOUCHRA BENKESSOU

Lead sponsor

Clinique du Trocadéro

Sponsor institution